{
  "id": 19067,
  "label": "folinic acid-responsive seizures",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019197",
  "properties": {
    "xrefs": [
      "GARD:0018938",
      "MEDGEN:908191",
      "Orphanet:79097",
      "SCTID:717276003",
      "UMLS:C4273952",
      "icd11.foundation:723504178"
    ],
    "synonyms": [
      "Folinic acid responsive seizures"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A very rare neonatal epileptic encephalopathy disorder characterized clinically by myoclonic and clonic, or clonic seizures associated with apnea occurring several hours to 5 days after birth and responding to folinic acid."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19114,
      "label": "metabolic disease involving other neurotransmitter deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018979",
          "MEDGEN:1843271",
          "Orphanet:79219",
          "UMLS:C5681275",
          "icd11.foundation:946446904"
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0019253"
    },
    {
      "id": 23787,
      "label": "metabolic epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6761
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1843497",
          "UMLS:C4524099"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Metabolic epilepsies are conceptualized as having a distinct metabolic abnormality that has been demonstrated to be associated with a substantially increased risk of developing epilepsy in appropriately designed studies. Metabolic disorders have genetic origin; however, the metabolic abnormalities are a separate disorder interposed between the genetic defect and the epilepsy."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100033"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19114,
      "label": "metabolic disease involving other neurotransmitter deficiency"
    },
    {
      "id": 23787,
      "label": "metabolic epilepsy"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}